Evidence mapPaperPMID 40478366Full record

ReviewThe Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology2025

Efficacy and safety of tafolecimab a new PCSK9 inhibitor in patients with hyperlipidemia: a systematic review and meta-analysis of randomized controlled trials.

Ali Ashraf Salah Ahmed, Ahmad Alkheder, Mohamed Ahmed Ali, Mohamed R Abdelraouf, Toka Ahmed Ashour, Hazem Mohamed Salamah, Abdelrahman Mahmoud, Diaa Hakim

Abstract readReview
In one paragraph

Review in The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Ali Ashraf Salah AhmedFaculty of Medicine, Minia University, Minia, Egypt.
Ahmad AlkhederDepartment of Otorhinolaryngology, Al Mouwasat University Hospital, Damascus University, Damascus, Syria.
Mohamed Ahmed AliQena Faculty of Medicine, South Valley University, Qena, Egypt. mohammedahmedalihassan2003@gmail.com.ORCID http://orcid.org/0000-0001-8142-8073
Mohamed R AbdelraoufFaculty of Medicine, Alexandria University, Alexandria, Egypt.
Toka Ahmed AshourFaculty of Medicine, Minia University, Minia, Egypt.
Hazem Mohamed SalamahFaculty of Medicine, Zagazig University, Zagazig, Egypt.
Abdelrahman MahmoudFaculty of Medicine, Minia University, Minia, Egypt.
Diaa HakimBrigham and Women's Hospital, Harvard Medical School, Boston, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHyperlipidemia is a common condition as nearly over 50% of adult Americans have high low-density lipoprotein (LDL) levels. Hyperlipidemia increases the risk of strokes, myocardial infarction, and other vascular events. PCSK9 monoclonal antibodies are one of the available options for the treatment of hyperlipidemia. Our study is a systematic review and meta-analysis that assesses the efficacy and safety of a new PCSK9 antibody, tafolecimab, in hyperlipidemia.

methodsSearching PubMed, EMBASE, Scopus, Web of Science (WOS), and Cochrane, we performed a PRISMA-based systematic review and meta-analysis to study effects of tafolecimab compared with placebo on different lipid indices that included LDL percent change, number of patients achieving ≥ 50% low-density lipoprotein cholesterol (LDL-C) reduction, LDL change from baseline, LDL change from baseline (CFB), apolipoprotein B CFB, and non-high-density lipoprotein cholesterol (non-HDL-C) CFB.

resultsFour randomized controlled trials (RCTs) with 1093 patients were included in our study; 709 (64.87%) of them were males. Tafolecimab reduced LDL percent change [mean difference (MD) = - 62.28, 95% confidence interval (CI) (- 65.21, -59.35), P < 0.00001], the number of patients achieving ≥ 50% LDL-C reduction [MD = 46.92, 95% CI (21.91, 103.9), P < 0.0001], LDL CFB [MD = - 73.58, 95% CI (- 83.13, -64.03), P < 0.001], non-HDL-C CFB [MD = - 82.21, 95% CI (- 86.65, - 77.77), P < 0.001], apolipoprotein B CFB [MD = - 52.01, 95% CI (- 54.86, - 49.17, P < 0.001]. No difference was detected in overall adverse events (AEs) [risk ratio (RR) = 0.94, 95% CI (0.88, 1.01), P = 0.1128], serous AEs [RR = 0.93, 95% CI (0.57, 1.52), P = 0.7799], and AEs leading to treatment discontinuation [RR = 2.58, 95% CI (0.76, 8.77), but yielded more injection site reactions [RR = 2.53, 95% CI (1.14, 5.63), P = 0.0222].

conclusionTafolecimab is a valuable treatment option for hyperlipidemia, which showed improvement in several lipid indices (LDL, LDL-C, LDL CFB, non-HDL-C CFB, and apolipoprotein B CFB). However, it increased the rates of injection site reactions.

Indexed as

AtherosclerosisHypercholesterolemiaHyperlipidemiaHyperlipoproteinemiaTafolecimab

Identifiers

PMID40478366
PMCPMC12144017

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.